_ , ...... =5 -;, .Core A will focus on biological evaluation of extracts, chromatograpnic'fractions,'and pure isolates preparedby all of the projects within the program in order to help prioritize subsequent biological and chemical work.This strategy of using bioassay-guided isolation will afford us the opportunity to pursue biological activitywithin complex mixtures. Extracts found active by Core A will be further purified by Projects 1-3 (OSU, UIC,and RTI, respectively) and the pure isolates returned to us for further analysis. Promising pure compoundswill ultimately be further tested in animal models to assess efficacy and toxicity. Mechanism of action studieswill be conduced to study the molecular pharmacology of pure compounds with the most favorabletherapeutic indices. The Leader of Core A has well-established collaborations with all of the Project Leadersof this Program Project and has previously employed a variety of assays for natural product drug discovery.Our ongoing working relationships with other Projects and Cores and our ability to develop new biologicalassays as needed will assure that Core A is fully integrated in the program project and serves all projectstherein.
The Specific Aims for Core A are to (1) conduct molecular-target based assays including the histonedeacetylase assay (HDAC) and inhibition of the 20S proteasome. These assays will be conducted initially onextract of materials Our second specific aim is to follow active leads identified by initial analysis using cellbased assays such as HL60, which is known to overexpress the 20S proteasome, or HeLa cells that are thesource of the HDAC used in the molecular target assays. Our third specific aim is to assess the activity ofour most promising active pure compounds in vivo. These experiments will include initial dose rangingstudies followed by efficacy studies using the hollow fiber assay or tumor xenografts studies inimmunodeficient mice. Finally, studies will be performed on those pure compounds that prove to be effectiveanticancer agents with limited toxicity. in mice. These studies will focus on determining the mechanism ofaction and may include studies such as pathway of apoptosis induction or mechanism of cell cycle arrest.The biological assays outlined in this Core, used in concert with Cores B through D, will provide a solidfoundation of support for all the Projects within the program.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
1P01CA125066-01A1
Application #
7302064
Study Section
Special Emphasis Panel (ZCA1-GRB-P (M1))
Project Start
2007-07-01
Project End
2012-06-30
Budget Start
2007-07-01
Budget End
2008-08-31
Support Year
1
Fiscal Year
2007
Total Cost
$240,109
Indirect Cost
Name
Ohio State University
Department
Type
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
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